What is NDC 0093-0010?

0093-0010 is the product NDC for Tolterodine Tartrate, Tolterodine tartrate 1 mg/1 tablet, film coated, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Tolterodine Tartrate?

31 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Tolterodine Tartrate NDC 0093-0010

NDC codes

FDA NDC Directory

Product NDC (as listed)0093-0010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00093-0010Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
0093-0010-06	0009300100600093001006	60 TABLET, FILM COATED in 1 BOTTLE (0093-0010-06)Marketed from Nov 1, 2015

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Tolterodine Tartrate
Generic name (nonproprietary): tolterodine tartrate
Active ingredients: Tolterodine tartrate — 1 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Teva Pharmaceuticals USA, Inc.NDC labeler code 0093
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077006
Marketing start: Nov 1, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers: Product ID 0093-0010_2f429822-d6d2-43c0-9aaf-1270b3e92a2fSPL ID 2f429822-d6d2-43c0-9aaf-1270b3e92a2fSPL set ID d27e25b5-5d02-419f-b098-41fb162c5872RxCUI 855178, 855194UNII 5T619TQR3R
Pharmacologic class: Cholinergic Muscarinic Antagonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N400093001006 followed by a unit qualifier and the quantity

Package 00093-0010-06. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Oct 11, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Tolterodine tablets are indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0093-0010

What is NDC 0093-0010?: 0093-0010 is the product NDC for Tolterodine Tartrate, Tolterodine tartrate 1 mg/1 tablet, film coated, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Tolterodine Tartrate.
What is the active ingredient?: Tolterodine tartrate.
Who is the labeler?: Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Tolterodine Tartrate?: 31 other product NDCs are listed under this name. See all Tolterodine Tartrate NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Tolterodine Tartrate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Tolterodine Tartrate	Tolterodine tartrate 2 mg/1	Capsule, Extended releaseOral	Major Pharmaceuticals	0904-7574	00904-7574-04
Tolterodine Tartrate	Tolterodine tartrate 4 mg/1	Capsule, Extended releaseOral	Major Pharmaceuticals	0904-7575	00904-7575-04
Tolterodine tartrate	Tolterodine tartrate 4 mg/1	Capsule, Extended releaseOral	Unichem Pharmaceuticals (USA), Inc.	29300-307	29300-0307-0529300-0307-1329300-0307-19
Tolterodine tartrate	Tolterodine tartrate 2 mg/1	Capsule, Extended releaseOral	Unichem Pharmaceuticals (USA), Inc.	29300-306	29300-0306-0529300-0306-1329300-0306-19
Tolterodine Tartrate	Tolterodine tartrate 2 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-806	31722-0806-0131722-0806-0231722-0806-05+1 more
Tolterodine Tartrate	Tolterodine tartrate 1 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-805	31722-0805-0131722-0805-0231722-0805-05+1 more
Tolterodine Tartrate	Tolterodine tartrate 2 mg/1	Capsule, Extended releaseOral	Slate Run Pharmaceuticals, LLC	70436-160	70436-0160-0270436-0160-0470436-0160-06
Tolterodine Tartrate	Tolterodine tartrate 4 mg/1	Capsule, Extended releaseOral	Slate Run Pharmaceuticals, LLC	70436-161	70436-0161-0270436-0161-0470436-0161-06
Tolterodine tartrate	Tolterodine tartrate 2 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-098	33342-0098-0933342-0098-1233342-0098-15
Tolterodine tartrate	Tolterodine tartrate 1 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-097	33342-0097-0933342-0097-1233342-0097-15

All 32 Tolterodine Tartrate NDCs

Other NDCs under ANDA 077006

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 077006
Product	Strength	Form · route	Labeler	Product NDC
Tolterodine Tartrate	Tolterodine tartrate 2 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals USA, Inc.	0093-0018
Tolterodine Tartrate	Tolterodine tartrate 1 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-319